Have questions? Visit https://www.reddit.com/r/SNPedia

rs4930103

From SNPedia

Orientationplus
Stabilizedplus
Make rs4930103(A;A)
Make rs4930103(A;G)
Make rs4930103(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2003314
is asnp
is mentioned by
dbSNPrs4930103
ebirs4930103
HLIrs4930103
Exacrs4930103
Varsomers4930103
Maprs4930103
PheGenIrs4930103
hapmaprs4930103
1000 genomesrs4930103
hgdprs4930103
ensemblrs4930103
gopubmedrs4930103
geneviewrs4930103
scholarrs4930103
googlers4930103
pharmgkbrs4930103
gwascentralrs4930103
openSNPrs4930103
23andMers4930103
23andMe allrs4930103
SNP Nexus

SNPshotrs4930103
SNPdbers4930103
MSV3drs4930103
GWAS Ctlgrs4930103
GMAF0.4536
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23725790]
Trait DNA methylation (parent-of-origin)
Title GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
Risk Allele A
P-val 5E-16
Odds Ratio NR NR


[PMID 16839189OA-icon.png] Human imprinted chromosomal regions are historical hot-spots of recombination.